Canonical Allele Identifier: CA2269942629

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63482546A= , CM000679.2:g.63482546A=	GRCh38
NC_000017.10:g.61559907A= , CM000679.1:g.61559907A=	GRCh37
NC_000017.9:g.58913639A=	NCBI36
NG_011648.1:g.10474A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.1199A= MANE Select	ENSP00000290866.4:p.Gln400=
ENST00000290866.9:c.1199A=	ENSP00000290866.4:p.Gln400=
ENST00000428043.5:c.1199A=	ENSP00000397593.2:p.Gln400=
ENST00000582678.5:c.*598A=	ENSP00000462995.1:n.*598A=
ENST00000584529.5:n.1233A=
NM_000789.3:c.1199A=	NP_000780.1:p.Gln400=
XM_005257110.1:c.650A=	XP_005257167.1:p.Gln217=
NM_000789.4:c.1199A= MANE Select	NP_000780.1:p.Gln400=
NM_001382700.1:c.632A=	NP_001369629.1:p.Gln211=
NM_001382701.1:c.347A=	NP_001369630.1:p.Gln116=